DR. WONJIN Hand Safer Sanigel

Manufacturer: BEAUTY SKIN.CO.,Ltd.
Effective date: 2020-05-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:10:34

Label at a glance#

ProductDR. WONJIN Hand Safer Sanigel

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR WONJIN Hand Safer SanigelDrug Facts

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75708-7502-2	2022-01-28	C162847	48780-1	d6a99b39-bf38-a426-e053-dadaa90af4c2	DR. WONJIN Hand Safer Sanigel 2 ml x 50 pces

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75708-7502-2	DR. WONJIN Hand Safer Sanigel	2 mL in 1 POUCH	GEL	2		1
75708-7502-2	DR. WONJIN Hand Safer Sanigel	50 in 1 BOX	GEL	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75708-7502	DR. WONJIN HAND SAFER SANIGEL (ETHANOL) GEL [BEAUTY SKIN.CO.,LTD.]	1	Legacy NDC, 2 package rows	20200510_a53a6c6e-88db-dd7a-e053-2995a90a20cb.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

DR. WONJIN Hand Safer Sanigel
Ethanol
LEMON
BUTYLENE GLYCOL
ALOE VERA LEAF
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
TROLAMINE
CENTELLA ASIATICA
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75708-7502	75708-7502-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LEMON	24RS0A988O	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	IACT
CENTELLA ASIATICA	7M867G6T1U	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a53a6c6e-88dc-dd7a-e053-2995a90a20cb			a53a6c6e-88db-dd7a-e053-2995a90a20cb	2020-05-09		Exact identifier spl id: a53a6c6e-88dc-dd7a-e053-2995a90a20cb spl set id: a53a6c6e-88db-dd7a-e053-2995a90a20cb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.